Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,542 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,542 in last 12 months

Showing 1702117040 of 51,038 recalls

DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Toposar (etoposide injection USP) Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 9, 2021· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...

The Issue: Customers were not notified of previous recalls associated with various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...

The Issue: Customers were not notified of previous recalls associated with various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...

The Issue: Customers were not notified of previous recalls associated with various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...

The Issue: Customers were not notified of previous recalls associated with various...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· In2Bones, SAS

Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...

The Issue: This Field Action is being conducted following identification of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Cardinal Health 200, LLC

Recalled Item: McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A Recalled by...

The Issue: Safety shield not locking into the cannula. If the safety shield activation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Cardinal Health 200, LLC

Recalled Item: Magellan 3 mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...

The Issue: Safety shield not locking into the cannula. If the safety shield activation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Cardinal Health 200, LLC

Recalled Item: Magellan Hypodermic Safety Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Safety shield not locking into the cannula. If the safety shield activation...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Meridian Bioscience Inc

Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...

The Issue: Use of the kits after incorrect storage could lead to a potential...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Mizuho OSI

Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...

The Issue: There is a potential that hand control units may cause the tabletop to slide...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 870 DR Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing